HuagongsheHuagongshe Chemistry Print Report · For research reference only
5-Chloro-2-fluoro-3-nitropyridine → 5-Chloro-2-fluoropyridin-3-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 5-Chloro-2-fluoro-3-nitropyridine | HCID 12275768 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 5-Chloro-2-fluoropyridin-3-amine | HCID 20042888 | 76.4% |
Reaction Steps
7.5 g (0.042 mol) of 5-chloro-2-fluoro-3-nitropyridine are dissolved in 80 ml of ethanol. This solution is hydrogenated with hydrogen, in the presence of 1 g of Raney nickel catalyst, under normal pressure and at a temperature in the range from 20° to 25° C. After a hydrogenation period of 20 hours, the catalyst is removed and the solvent is evaporated off. The residue is taken up in ethyl acetate and the resultant solution is filtered through a layer of silica gel. The solvent is evaporated off and the residue is triturated in hexane. The precipitate is subsequently filtered and dried, affording 4.7 g (76%) of 3-amino-5-chloro-2-fluoropyridine, m.p. 74° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04831148 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-2e2791366d20469bbd666d7609e23186 |
| Source note | uspto-grants-1989_05 |